The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
86801912 8680191 2 F 201007 20160728 20120724 20160802 EXP US-009507513-1207USA007175 MERCK 0.00 F Y 0.00000 20160802 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
86801912 8680191 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral UNK UNK, UNKNOWN U 20560 TABLET
86801912 8680191 2 SS FOSAMAX PLUS D ALENDRONATE SODIUMCHOLECALCIFEROL 1 Oral UNK, UNKNOWN U 0 TABLET
86801912 8680191 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral UNK, UNKNOWN U 20560 TABLET
86801912 8680191 4 SS RECLAST ZOLEDRONIC ACID 1 Unknown UNK UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86801912 8680191 1 Osteoporosis
86801912 8680191 2 Osteoporosis
86801912 8680191 3 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
86801912 8680191 DS
86801912 8680191 OT
86801912 8680191 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
86801912 8680191 Anaemia postoperative
86801912 8680191 Biopsy bone abnormal
86801912 8680191 Femur fracture
86801912 8680191 Leukopenia
86801912 8680191 Rheumatoid arthritis
86801912 8680191 Thrombocytopenia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
86801912 8680191 1 199807 2010 0
86801912 8680191 2 199807 2010 0
86801912 8680191 3 199807 2010 0
86801912 8680191 4 199807 2010 0